Available courses

Introduction to Clinical Research

Course categoryClinical Research

This course provides a comprehensive introduction to the pharmaceutical and clinical research industry, its history, and key milestones. Learners will explore the roles and responsibilities of stakeholders, ethical foundations, and global regulatory frameworks governing clinical trials. Core principles of Good Clinical Practice (GCP) are emphasized, along with essential trial processes and documentation. The course also covers emerging technologies in trial management and the importance of safety reporting. Designed as a foundation, it prepares learners for deeper study in advanced clinical research concepts and practices.

Epidemiology and Evidence-Based Medicine

Course categoryClinical Research

This course introduces the core concepts of epidemiology and the practice of evidence-based medicine (EBM). It covers measures of disease frequency, study designs, causation, and key statistical tools for health research. Learners will explore the five steps of EBM—asking, acquiring, appraising, applying, and assessing evidence. Ethical considerations, historical milestones, and case studies are included to build context. By the end, participants will be able to critically evaluate medical literature and apply evidence to improve patient care and public health.

Pharmaceutical Medicine

Course categoryClinical Research

This comprehensive course provides an in-depth understanding of the pharmaceutical and clinical research landscape, covering the complete drug development lifecycle from pre-clinical research to post-marketing safety. Learners will explore clinical trial design, endpoints, registries, pediatric and pregnancy safety considerations, and emerging areas such as stem cell research, genetics, and personalized medicine. The course integrates regulatory frameworks, ethical principles, and industry best practices to ensure real-world relevance. Designed for life-science and healthcare professionals, this course builds both conceptual clarity and practical insight into modern pharmaceutical medicine.

Ethics in Clinical Research

Course categoryClinical Research

This course provides a comprehensive overview of Ethics in Clinical Research, covering the ethical foundations, regulatory frameworks, and practical applications essential for conducting responsible clinical studies. It explores core ethical principles, historical milestones, and international guidelines governing human subject research. Learners will gain in-depth understanding of informed consent, participant protection, and ethical decision-making across different trial phases. The course also addresses global and national regulations, including harmonization guidelines and country-specific requirements.

Roles and Responsibilities in Clinical Research

Course categoryClinical Research

This course explains the key roles and responsibilities of all major stakeholders involved in clinical research. It covers the duties of investigators, sponsors, vendors, IRBs, and clinical research staff, with a strong focus on ethics, compliance, and regulatory requirements. Learners will understand how these roles work together to protect study participants and ensure data quality. The course also highlights Good Clinical Practice (GCP) principles and applicable guidelines. It is designed to give professionals a clear and practical understanding of accountability throughout the clinical trial process.